Riik: Ameerika Ühendriigid
keel: inglise
Allikas: NLM (National Library of Medicine)
IRBESARTAN (UNII: J0E2756Z7N) (IRBESARTAN - UNII:J0E2756Z7N), HYDROCHLOROTHIAZIDE (UNII: 0J48LPH2TH) (HYDROCHLOROTHIAZIDE - UNII:0J48LPH2TH)
Unichem Pharmaceuticals (USA), Inc.
IRBESARTAN
IRBESARTAN 150 mg
ORAL
PRESCRIPTION DRUG
Irbesartan and hydrochlorothiazide tablets, USP are indicated for the treatment of hypertension. Irbesartan and hydrochlorothiazide tablets, USP may be used in patients whose blood pressure is not adequately controlled on monotherapy. Irbesartan and hydrochlorothiazide tablets, USP may also be used as initial therapy in patients who are likely to need multiple drugs to achieve their blood pressure goals. The choice of irbesartan and hydrochlorothiazide tablets as initial therapy for hypertension should be based on an assessment of potential benefits and risks. Patients with stage 2 (moderate or severe) hypertension are at relatively high risk for cardiovascular events (such as strokes, heart attacks, and heart failure), kidney failure, and vision problems, so prompt treatment is clinically relevant. The decision to use a combination as initial therapy should be individualized and may be shaped by considerations such as the baseline blood pressure, the target goal, and the incremental likelihood of achieving g
Irbesartan and Hydrochlorothiazide Tablets USP, 150 mg/12.5 mg are peach colored, biconvex, round, film-coated tablets with "U" debossed on one side and "7" on other side. Bottles of 30: NDC 29300-215-13 Bottles of 90: NDC 29300-215-19 Bottles of 1,000: NDC 29300-215-10 Irbesartan and Hydrochlorothiazide Tablets USP, 300 mg/12.5mg are peach colored, biconvex, oval, film-coated tablets with "U" debossed on one side and "71" on other side. Bottles of 30: NDC 29300-216-13 Bottles of 90: NDC 29300-216-19 Bottles of 1,000: NDC 29300-216-10 Store at 20o to 25o C (68o to 77o F) [see USP controlled Room Temperature].
Abbreviated New Drug Application
IRBESARTAN AND HYDROCHLOROTHIAZIDE - IRBESARTAN AND HYDROCHLOROTHIAZIDE TABLET, FILM COATED UNICHEM PHARMACEUTICALS (USA), INC. ---------- HIGHLIGHTS OF PRESCRIBING INFORMATION THESE HIGHLIGHTS DO NOT INCLUDE ALL THE INFORMATION NEEDED TO USE IRBESARTAN AND HYDRCHLOROTHIAZIDE TABLETS SAFELY AND EFFECTIVELY. SEE FULL PRESCRIBING INFORMATION FOR IRBESARTAN AND HYDRCHLOROTHIAZIDE TABLETS. IRBESARTAN AND HYDRCHLOROTHIAZIDE TABLETS, FOR ORAL USE. INITIAL U.S. APPROVAL: 1997 WARNING: FETAL TOXICITY _SEE FULL PRESCRIBING INFORMATION FOR COMPLETE BOXED WARNING._ WHEN PREGNANCY IS DETECTED, DISCONTINUE IRBESARTAN AND HYDROCHLOROTHIAZIDETABLETS AS SOON AS POSSIBLE. (5.1, 8.1) DRUGS THAT ACT DIRECTLY ON THE RENIN-ANGIOTENSIN SYSTEM CAN CAUSE INJURY AND DEATH TO THE DEVELOPING FETUS. (5.1, 8.1) RECENT MAJOR CHANGES Warnings and Precautions (5.8) 5/2021 INDICATIONS AND USAGE Irbesartan and hydrochlorothiazide tablets are a combination of irbesartan, an angiotensin II receptor antagonist, and hydrochlorothiazide, a thiazide diuretic, indicated for hypertension: In patients not adequately controlled with monotherapy. (1) As initial therapy in patients likely to need multiple drugs to achieve their blood pressure goals. (1) DOSAGE AND ADMINISTRATION GENERAL CONSIDERATIONS Maximum effects within 2 to 4 weeks after dose change. (2.1) Renal impairment: Not recommended for patients with severe renal impairment (creatinine clearance <30 mL/min). (2.1, 5.8) HYPERTENSION Initiate with 150 mg/12.5 mg. Titrate to 300 mg/12.5 mg then 300 mg/25 mg if needed. (2.2) Replacement therapy: May be substituted for titrated components. (2.3) DOSAGE FORMS AND STRENGTHS 150 mg irbesartan/12.5 mg hydrochlorothiazide tablets (3) 300 mg irbesartan/12.5 mg hydrochlorothiazide tablets (3) CONTRAINDICATIONS Hypersensitivity to any component of this product (4) Anuria (4) Hypersensitivity to sulfonamide-derived drugs (4) Do not coadminister aliskiren with irbesartan and hydrochlorothiazide tablets in patients with diabetes (4) WARNINGS AND PRECAUTIONS Hypo Lugege kogu dokumenti